• Gatti, Teresa
• Schmitz, Fabian
• Horn, Jonas
• Schlettwein, Derck
• Sann, Joachim
• Gerhard, Marina
• Neisius, Raphael

Abstract

<jats:title>Abstract</jats:title><jats:p>Silver-bismuth double perovskites are promising replacement materials for lead-based ones in photovoltaic (PV) devices due to the lower toxicity and enhanced stability to environmental factors. In addition, they might even be more suitable for indoor PV, due to the size of their bandgap better matching white LEDs emission. Unfortunately, their optoelectronic performance does not reach that of the lead-based counterparts, because of the indirect nature of the band gap and the high exciton binding energy. One strategy to improve the electronic properties is the dimensional reduction from the 3D to the 2D perovskite structure, which features a direct band gap, as it has been reported for 2D monolayer derivates of Cs<jats:sub>2</jats:sub>AgBiBr<jats:sub>6</jats:sub> obtained by substituting Cs<jats:sup>+</jats:sup> cations with bulky alkylammonium cations. However, a similar dimensional reduction also brings to a band gap opening, limiting light absorption in the visible. In this work, we report on the achievement of a bathochromic shift in the absorption features of a butylammonium-based silver-bismuth bromide monolayer double perovskite through doping with iodide and study the optical properties and stability of the resulting thin films in environmental conditions. These species might constitute the starting point to design future sustainable materials to implement as active components in indoor photovoltaic devices used to power the IoT.</jats:p>

Topics

• perovskite
• impedance spectroscopy
• silver
• thin film
• toxicity
• Bismuth